Department of Science, Section of Biomedical Sciences and Technologies, University "Roma Tre", Rome, Italy.
Department of Physiology and Pharmacology, Sapienza, University of Rome, Rome, Italy; Hotchkiss Brain Institute, Departments of Cell Biology and Anatomy and Psychiatry, University of Calgary, Calgary, AB, Canada.
Eur Neuropsychopharmacol. 2015 Aug;25(8):1362-74. doi: 10.1016/j.euroneuro.2015.04.005. Epub 2015 Apr 14.
To date, our understanding of the relative contribution and potential overlapping roles of the endocannabinoids anandamide (AEA) and 2-arachidonoylglycerol (2-AG) in the regulation of brain function and behavior is still limited. To address this issue, we investigated the effects of systemic administration of JZL195, that simultaneously increases AEA and 2-AG signaling by inhibiting their hydrolysis, in the regulation of socio-emotional behavior in adolescent and adult rats. JZL195, administered at the dose of 0.01mg/kg, increased social play behavior, that is the most characteristic social activity displayed by adolescent rats, and increased social interaction in adult animals. At both ages, these behavioral effects were antagonized by the CB1 cannabinoid receptor antagonist SR141716A and were associated with increased brain levels of 2-AG, but not AEA. Conversely, at the dose of 1mg/kg, JZL195 decreased general social exploration in adolescent rats without affecting social play behavior, and induced anxiogenic-like effects in the elevated plus-maze test both in adolescent and adult animals. These effects, mediated by activation of CB1 cannabinoid receptors, were paralleled by simultaneous increase in AEA and 2-AG levels in adolescent rats, and by an increase of only 2-AG levels in adult animals. These findings provide the first evidence for a role of 2-AG in social behavior, highlight the different contributions of AEA and 2-AG in the modulation of emotionality at different developmental ages and suggest that pharmacological inhibition of AEA and 2-AG hydrolysis is a useful approach to investigate the role of these endocannabinoids in neurobehavioral processes.
迄今为止,我们对于内源性大麻素大麻素(AEA)和 2-花生四烯酸甘油(2-AG)在调节大脑功能和行为方面的相对贡献和潜在重叠作用的理解仍然有限。为了解决这个问题,我们研究了全身性给予 JZL195(一种同时通过抑制其水解来增加 AEA 和 2-AG 信号的化合物)对青少年和成年大鼠社会情感行为的调节作用。JZL195 的剂量为 0.01mg/kg 时,增加了社会玩耍行为(这是青少年大鼠表现出的最典型的社交活动)和成年动物的社交互动。在这两个年龄段,这些行为效应均被 CB1 大麻素受体拮抗剂 SR141716A 拮抗,并且与脑内 2-AG 水平升高有关,但与 AEA 无关。相反,在 1mg/kg 的剂量下,JZL195 减少了青少年大鼠的一般社交探索行为,而不影响社交玩耍行为,并且在青少年和成年动物的高架十字迷宫测试中引起焦虑样效应。这些效应由 CB1 大麻素受体的激活介导,与青少年大鼠中 AEA 和 2-AG 水平的同时升高有关,而与成年动物中仅 2-AG 水平的升高有关。这些发现为 2-AG 在社会行为中的作用提供了首个证据,强调了 AEA 和 2-AG 在不同发育年龄调节情感方面的不同贡献,并表明抑制 AEA 和 2-AG 水解的药理学方法是研究这些内源性大麻素在神经行为过程中作用的有用方法。